The field of public health has witnessed substantial advancements in medical knowledge and technology, contributing to a notable increase in human life expectancy. While these advancements have extended lives, they have not proportionately enhanced the quality of life, especially in the crucial end-of-life stages. This disparity highlights significant challenges in addressing person-centered care during life-limiting conditions, which often lack adequate attention within broader healthcare goals.
This Research Topic is focused on driving a comprehensive revaluation of person-centered care, specifically emphasizing the nuances of end-of-life scenarios often faced by individuals with severe illnesses. The objective is to improve both the quality of life for patients and the well-being of caregivers, consequently lightening the burden on global health systems. By concentrating on end-of-life care aspects, such as patient engagement, caregiver support, hospital readmissions, advocacy for advance directives, and the growth of palliative and hospice care, research can foster meaningful change.
The scope of this research topic will include an examination of the current methods used to measure the quality of end-of-life care, such as international ranking systems. Despite providing a comparative framework across countries, there remains a debate surrounding these metrics and their applicability across differing cultural, political, and moral landscapes. Through a dual analytical approach, encompassing both quantitative and qualitative angles, this research aims to uncover key factors in care performance. The insights garnered will inform policy reforms and the development of superior intervention strategies, integrating principles from Aging and Public Health, Public Health Policy, and Life-Course Epidemiology.
To gather further insights, we welcome articles addressing, but not limited to, the following themes:
Patient engagement strategies in end-of-life care
Caregiver support frameworks and their impact
International comparisons of end-of-life care quality metrics
The role of public health policy in shaping palliative care
Lived experiences of patients and caregivers in the end-of-life stage
Compassionate engagement of communities in support of palliative and end-of-life care
We encourage submissions that explore these multifaceted aspects of end-of-life care to drive forward improvements in societal approaches to aging and terminal diseases, ensuring dignity and quality in the final chapters of life.
Article types and fees
This Research Topic accepts the following article types, unless otherwise specified in the Research Topic description:
Brief Research Report
Clinical Trial
Community Case Study
Conceptual Analysis
Curriculum, Instruction, and Pedagogy
Data Report
Editorial
FAIR² Data
FAIR² DATA Direct Submission
Articles that are accepted for publication by our external editors following rigorous peer review incur a publishing fee charged to Authors, institutions, or funders.
Article types
This Research Topic accepts the following article types, unless otherwise specified in the Research Topic description:
Brief Research Report
Clinical Trial
Community Case Study
Conceptual Analysis
Curriculum, Instruction, and Pedagogy
Data Report
Editorial
FAIR² Data
FAIR² DATA Direct Submission
General Commentary
Hypothesis and Theory
Methods
Mini Review
Opinion
Original Research
Perspective
Policy and Practice Reviews
Policy Brief
Review
Study Protocol
Systematic Review
Technology and Code
Keywords: Person-centered care, End-of-life care, Quality of life, Palliative care, Public health policy
Important note: All contributions to this Research Topic must be within the scope of the section and journal to which they are submitted, as defined in their mission statements. Frontiers reserves the right to guide an out-of-scope manuscript to a more suitable section or journal at any stage of peer review.